Related Experiment Video
Updated: Jul 2, 2025

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
LPL rs264, PROCR rs867186 and PDGF rs974819 Gene Polymorphisms in Patients with Unstable Angina
Damian Malinowski1, Krzysztof Safranow2, Andrzej Pawlik3
1Department of Pharmacokinetics and Therapeutic Drug Monitoring, Pomeranian Medical University, 70-111 Szczecin, Poland.
Insights
Genetic variations in LPL, PROCR, and PDGF were not linked to unstable angina risk. However, PROCR rs867186 and PDGF rs974819 gene polymorphisms may influence lipid metabolism parameters in patients.
Area of Science:
- Cardiovascular Genetics
- Molecular Cardiology
- Lipid Metabolism
Background:
- Coronary artery disease (CAD) involves atherosclerosis and thrombosis, influenced by inflammation and immune responses.
- Lipids and coagulation are key in CAD pathogenesis, prompting research into related genes.
- Lipoprotein lipase (LPL), Protein C (PC), and Platelet-derived growth factor (PDGF) influence lipid metabolism and coagulation, potentially impacting CAD risk.
Purpose of the Study:
- To investigate associations between LPL rs264, PROCR rs867186, and PDGF rs974819 gene polymorphisms and unstable angina risk.
- To explore relationships between these polymorphisms and clinical parameters in unstable angina patients.
Main Methods:
- Study included 232 unstable angina patients and 144 healthy controls.
- Genotyping for LPL rs264, PROCR rs867186, and PDGF rs974819 polymorphisms was performed using real-time PCR.
Main Results:
- No significant differences in polymorphism distribution were found between unstable angina patients and controls.
- PROCR rs867186 and PDGF rs974819 polymorphisms showed associations with specific clinical parameters.
- PDGF rs974819 CC genotype correlated with higher cholesterol and LDL levels.
- PROCR rs867186 AA genotype was associated with lower HDL levels.
Conclusions:
- LPL rs264, PROCR rs867186, and PDGF rs974819 polymorphisms are not significant risk factors for unstable angina in this population.
- PDGF rs974819 and PROCR rs867186 polymorphisms may be associated with lipid metabolism parameters.
Background:
Coronary artery disease is caused by changes in the coronary arteries due to the atherosclerotic process and thrombotic changes. A very important role in the development of the atherosclerotic process in the coronary vessels is played by the inflammatory process and the immune response. Due to the important role of lipids and the coagulation process in the atherosclerotic process, research has also focused on genes affecting lipid metabolism and the coagulation system. Lipoprotein lipase (LPL) is an enzyme that metabolises lipids, hydrolysing triglycerides to produce free fatty acids and glycerol. Protein C (PC) is an essential component of coagulation and fibrinolysis. It is activated on the endothelial surface by the membrane-bound thrombin-thrombomodulin complex. Platelet-derived growth factor (PDGF) has a number of important functions in processes related to fibroblast and smooth muscle cell function. Due to their influence on lipid metabolism and coagulation processes, LPL, PROCR (endothelial cell protein C receptor) and PDGF may affect the atherosclerotic process and, thus, the risk of coronary heart disease. The aim of the study was to examine the associations between the LPL rs264, PROCR rs867186 and PDGF rs974819 gene polymorphisms and the risk of unstable angina and selected clinical parameters.
Methods:
The study included 232 patients with unstable angina and 144 healthy subjects as the control group. Genotyping was performed using real-time PCR.
Results:
There were no statistically significant differences in the distribution of the polymorphisms tested between the patients with unstable angina and the control subjects. The results showed associations between the PROCR rs867186 and PDGF rs974819 polymorphisms and some clinical parameters in patients with unstable angina. In patients with the PDGF rs974819 CC genotype, there were increased values for cholesterol and LDL serum levels in comparison with patients with the PDGF rs974819 CT and TT genotypes. In patients with the PROCR rs867186 AA genotype, HDL serum levels were lower than in patients with the GA genotype.
Conclusions:
The results of our study did not show that the LPL rs264, PROCR rs867186 and PDGF rs974819 gene polymorphisms were significant risk factors for unstable angina in our population. The results of the study suggest that PDGF rs974819 and PROCR rs867186 may be associated with some parameters of lipid metabolism.
More Related Videos
06:21Author Spotlight: Genetic Profiling for Fluorouracil Response in Gastric Cancer
Published on: May 10, 2024
18:11A Research Method For Detecting Transient Myocardial Ischemia In Patients With Suspected Acute Coronary Syndrome Using Continuous ST-segment Analysis
Published on: December 28, 2012
Related Concept Videos
Antianginal Drugs: Nitrates and β-Blockers
Organic nitrates, such as nitroglycerin, play a pivotal role. Once metabolized, they liberate nitric oxide, a molecular marvel. Nitric oxide triggers guanylyl cyclase and augments cGMP production. This biochemical cascade orchestrates the relaxation of vascular smooth muscles, ushering in vasodilation and enhancing coronary blood flow....
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
Single Nucleotide Polymorphisms-SNPs
Multiple Allele Traits
Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...